VITATHYL
K-Number: K830105 · 1983-03-01
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Device Summary
Frequently Asked Questions
What is the VITATHYL?
VITATHYL is a medical device that received FDA 510(k) clearance on 1983-03-01. The listed applicant is North Pacific Dental, Inc.. The 510(k) number is K830105.
When did VITATHYL receive FDA 510(k) clearance?
VITATHYL received FDA 510(k) clearance on 1983-03-01, under 510(k) number K830105.
Who is the listed applicant for VITATHYL?
The FDA 510(k) record lists North Pacific Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITATHYL?
The FDA product code for VITATHYL is EAT.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing North Pacific Dental, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EAT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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